Cross-Sectional Study to Determine Distribution of Genetic Variants Among Subjects at Risk of, or With Known Non-alcoholic Steatohepatitis (NASH)
Cross-Sectional Study to Determine Distribution of Genetic Variants Among Subjects at Risk of, or With Known Non-alcoholic Steatohepatitis (NASH)
Collection of clinical and genetic data to help identify individuals that carry genetic variants of known importance in Non-alcoholic Steatohepatitis (NASH)
Key Inclusion Criteria:
One or more of the following:
A prior diagnosis of NASH with a Clinical Research Network (CRN) fibrosis score of F1 to F4 based on liver biopsy
Evidence of NAFLD by imaging or liver histology as described in the protocol
Known high-risk genotype for HSD17B13 (T/T or T/TA) and/or PNPLA3 (C/G,or G/G)
A clinical suspicion of NASH based on presence of 2 or more elements of the metabolic syndrome defined by:
Key Exclusion Criteria:
Note: Other protocol-defined Inclusion/ Exclusion Criteria apply
Philadelphia, Pennsylvania 19104, United States
Porto Alegre, Rio Grande do Sul 90430-001, Brazil
São Paulo, 05403-000, Brazil
Miguel Hidalgo, Mexico City 11650, Mexico
Dalseo-gu, Daegu 42601, South Korea
Seongnam-si, Gyeonggi-do 13620, South Korea
Seoul, Gyeonggi-do 04763, South Korea
Dongjak-gu, Seoul 06973, South Korea
Jongno-gu, Seoul 03080, South Korea